Soft Polymeric Matrix as a Macroscopic Cage for Magnetically Modulating Reversible Nanoscale Ligand Presentation

被引:35
作者
Wong, Siu Hong Dexter [1 ]
Wong, Wai Ki Ricky [1 ]
Lai, Chun Him Nathanael [1 ]
Oh, Jiwon [1 ]
Li, Zhuo [1 ]
Chen, Xiaoyu [1 ]
Yuan, Weihao [1 ]
Bian, Liming [1 ,2 ,3 ,4 ]
机构
[1] Chinese Univ Hong Kong, Dept Biomed Engn, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Shenzhen Res Inst, Shatin, Hong Kong, Peoples R China
[3] China Orthoped Regenerat Med Grp CORMed, Hangzhou 310058, Zhejiang, Peoples R China
[4] Chinese Univ Hong Kong, Ctr Novel Biomat, Shatin, Hong Kong 100097, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogel Functionalization; Matrix Hindrance; Magnetic Manipulation; Dynamic Cell Adhesion; Stem Cell differentiation; CELL-ADHESION; DIFFERENTIATION; BIOMATERIALS; POLARIZATION; SURFACES;
D O I
10.1021/acs.nanolett.9b05315
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A physical, noninvasive, and reversible means of controlling the nanoscale presentation of bioactive ligands is highly desirable for regulating and investigating the time-dependent responses of cells, including stem cells. Herein we report a magnetically actuated dynamic cell culture platform consisting of a soft hydrogel substrate conjugated with RGD-bearing magnetic nanoparticle (RGD-MNP). The downward/upward magnetic attraction conceals/promotes the presentation of the RGD-MNP in/on the soft hydrogel matrix, thereby inhibiting/enhancing the cell adhesion and mechanosensing-dependent differentiation. Meanwhile, the lateral magnetic attraction promotes the unidirectional migration of cells in the opposite direction on the hydrogel. Furthermore, cyclic switching between the "Exposed" and "Hidden" conditions induces the repeated cycles of differentiation/dedifferentiation of hMSCs which significantly enhances the differentiation potential of hMSCs. Our design approach capitalizes on the bulk biomaterial matrix as the macroscopic caging structure to enable dynamic regulation of cell-matrix interactions reversibly, which is hard to achieve by using conventional cell culture systems.
引用
收藏
页码:3207 / 3216
页数:10
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